A citation-based method for searching scientific literature

Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov, Ludo A M Broos, Angelita Tottene, Zhenyu Gao, Mariann Fodor, Chris I De Zeeuw, Rune R Frants, Nikolaus Plesnila, Jaap J Plomp, Daniela Pietrobon, Michel D Ferrari. Ann Neurol 2010
Times Cited: 152







List of co-cited articles
1499 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
467
67

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
45

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
223
44

Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.
Katharina Eikermann-Haerter, Ergin Dileköz, Chiho Kudo, Sean I Savitz, Christian Waeber, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. J Clin Invest 2009
192
38

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
133
37

Migraine pathophysiology: lessons from mouse models and human genetics.
Michel D Ferrari, Roselin R Klever, Gisela M Terwindt, Cenk Ayata, Arn M J M van den Maagdenberg. Lancet Neurol 2015
209
31

Pathophysiology of migraine.
Daniela Pietrobon, Michael A Moskowitz. Annu Rev Physiol 2013
370
29

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
647
28

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model.
Hayrunnisa Bolay, Uwe Reuter, Andrew K Dunn, Zhihong Huang, David A Boas, Michael A Moskowitz. Nat Med 2002
788
26

Spreading depression triggers headache by activating neuronal Panx1 channels.
Hulya Karatas, Sefik Evren Erdener, Yasemin Gursoy-Ozdemir, Sevda Lule, Emine Eren-Koçak, Zümrüt Duygu Sen, Turgay Dalkara. Science 2013
276
24

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
236
23

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
A H Stam, G-J Luijckx, B T Poll-Thé, I B Ginjaar, R R Frants, J Haan, M D Ferrari, G M Terwindt, A M J M van den Maagdenberg. J Neurol Neurosurg Psychiatry 2009
67
34

Casein kinase iδ mutations in familial migraine and advanced sleep phase.
K C Brennan, Emily A Bates, Robert E Shapiro, Jekaterina Zyuzin, William C Hallows, Yong Huang, Hsien-Yang Lee, Christopher R Jones, Ying-Hui Fu, Andrew C Charles,[...]. Sci Transl Med 2013
125
23

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
540
23


Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.
Katharina Eikermann-Haerter, Izumi Yuzawa, Tao Qin, Yumei Wang, Kwangyeol Baek, Young Ro Kim, Ulrike Hoffmann, Ergin Dilekoz, Christian Waeber, Michel D Ferrari,[...]. J Neurosci 2011
88
25

Mechanisms of migraine aura revealed by functional MRI in human visual cortex.
N Hadjikhani, M Sanchez Del Rio, O Wu, D Schwartz, D Bakker, B Fischl, K K Kwong, F M Cutrer, B R Rosen, R B Tootell,[...]. Proc Natl Acad Sci U S A 2001
953
22

Suppression of cortical spreading depression in migraine prophylaxis.
Cenk Ayata, Hongwei Jin, Chiho Kudo, Turgay Dalkara, Michael A Moskowitz. Ann Neurol 2006
404
21


Activation of central trigeminovascular neurons by cortical spreading depression.
Xichun Zhang, Dan Levy, Vanessa Kainz, Rodrigo Noseda, Moshe Jakubowski, Rami Burstein. Ann Neurol 2011
220
18



Activation of meningeal nociceptors by cortical spreading depression: implications for migraine with aura.
Xichun Zhang, Dan Levy, Rodrigo Noseda, Vanessa Kainz, Moshe Jakubowski, Rami Burstein. J Neurosci 2010
224
17

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression.
Katharina Eikermann-Haerter, Izumi Yuzawa, Ergin Dilekoz, Anne Joutel, Michael A Moskowitz, Cenk Ayata. Ann Neurol 2011
71
23


Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2.
Clizia Capuani, Marcello Melone, Angelita Tottene, Luca Bragina, Giovanna Crivellaro, Mirko Santello, Giorgio Casari, Fiorenzo Conti, Daniela Pietrobon. EMBO Mol Med 2016
68
25

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
139
16

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.
Angelita Tottene, Francesca Pivotto, Tommaso Fellin, Tiziana Cesetti, Arn M J M van den Maagdenberg, Daniela Pietrobon. J Biol Chem 2005
102
16

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.
L L Thomsen, M K Eriksen, S F Roemer, I Andersen, J Olesen, M B Russell. Brain 2002
152
16

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
183
16



The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
371
15

Clinical relevance of cortical spreading depression in neurological disorders: migraine, malignant stroke, subarachnoid and intracranial hemorrhage, and traumatic brain injury.
Martin Lauritzen, Jens Peter Dreier, Martin Fabricius, Jed A Hartings, Rudolf Graf, Anthony John Strong. J Cereb Blood Flow Metab 2011
460
15

Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizations.
Katharina Eikermann-Haerter, Jeong Hyun Lee, Izumi Yuzawa, Christina H Liu, Zhipeng Zhou, Hwa Kyoung Shin, Yi Zheng, Tao Qin, Tobias Kurth, Christian Waeber,[...]. Circulation 2012
114
15

Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i.
Mariano N Di Guilmi, Tiantian Wang, Carlota Gonzalez Inchauspe, Ian D Forsythe, Michel D Ferrari, Arn M J M van den Maagdenberg, J Gerard G Borst, Osvaldo D Uchitel. J Neurosci 2014
31
48

Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.
Paul J Adams, Ravi L Rungta, Esperanza Garcia, Arn M J M van den Maagdenberg, Brian A MacVicar, Terrance P Snutch. Proc Natl Acad Sci U S A 2010
47
29

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
14

Behavioral evidence for photophobia and stress-related ipsilateral head pain in transgenic Cacna1a mutant mice.
Mona Lisa Chanda, Alexander H Tuttle, Inna Baran, Cori Atlin, Daniella Guindi, Georgia Hathaway, Nyrie Israelian, Jeremy Levenstadt, Daniel Low, Lynn Macrae,[...]. Pain 2013
52
26

Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.
Zhenyu Gao, Boyan Todorov, Curtis F Barrett, Stijn van Dorp, Michel D Ferrari, Arn M J M van den Maagdenberg, Chris I De Zeeuw, Freek E Hoebeek. J Neurosci 2012
64
21

Calcium channels and migraine.
Daniela Pietrobon. Biochim Biophys Acta 2013
44
31

Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Verneri Anttila, Bendik S Winsvold, Padhraig Gormley, Tobias Kurth, Francesco Bettella, George McMahon, Mikko Kallela, Rainer Malik, Boukje de Vries, Gisela Terwindt,[...]. Nat Genet 2013
242
14

Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
13


Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
Verneri Anttila, Hreinn Stefansson, Mikko Kallela, Unda Todt, Gisela M Terwindt, M Stella Calafato, Dale R Nyholt, Antigone S Dimas, Tobias Freilinger, Bertram Müller-Myhsok,[...]. Nat Genet 2010
249
11

Migraine: a disorder of brain excitatory-inhibitory balance?
Dania Vecchia, Daniela Pietrobon. Trends Neurosci 2012
143
11

Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice.
Katharina Eikermann-Haerter, Michael J Baum, Michel D Ferrari, Arn M J M van den Maagdenberg, Michael A Moskowitz, Cenk Ayata. Ann Neurol 2009
70
15

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.
K Jurkat-Rott, T Freilinger, J P Dreier, J Herzog, H Göbel, G C Petzold, P Montagna, T Gasser, F Lehmann-Horn, M Dichgans. Neurology 2004
113
11

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
M-J Castro, A H Stam, C Lemos, B de Vries, K R J Vanmolkot, J Barros, G M Terwindt, R R Frants, J Sequeiros, M D Ferrari,[...]. Cephalalgia 2009
64
17



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.